Christina Hung

1.1k total citations
21 papers, 370 citations indexed

About

Christina Hung is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, Christina Hung has authored 21 papers receiving a total of 370 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 10 papers in Physiology and 9 papers in Genetics. Recurrent topics in Christina Hung's work include Lysosomal Storage Disorders Research (10 papers), Genomics and Rare Diseases (7 papers) and Trypanosoma species research and implications (5 papers). Christina Hung is often cited by papers focused on Lysosomal Storage Disorders Research (10 papers), Genomics and Rare Diseases (7 papers) and Trypanosoma species research and implications (5 papers). Christina Hung collaborates with scholars based in United States, Austria and Canada. Christina Hung's co-authors include Olaf A. Bodamer, Maria Rita Passos‐Bueno, Jacek Pilch, Somayyeh Fahiminiya, Mayana Zatz, Guilherme Lopes Yamamoto, Anna Abramowicz, Jacek Majewski, Ingrid Cristian and Meire Aguena and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and The FASEB Journal.

In The Last Decade

Christina Hung

18 papers receiving 362 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Christina Hung United States 11 223 101 87 84 55 21 370
Prajnya Ranganath India 11 150 0.7× 84 0.8× 21 0.2× 115 1.4× 50 0.9× 56 367
Guy H. Grayson United States 5 89 0.4× 193 1.9× 69 0.8× 24 0.3× 70 1.3× 7 393
Petra Kapaun Germany 7 73 0.3× 157 1.6× 39 0.4× 49 0.6× 62 1.1× 7 331
Hagit Baris Feldman Israel 11 131 0.6× 67 0.7× 34 0.4× 71 0.8× 31 0.6× 42 366
C. E. Hatton United Kingdom 9 157 0.7× 337 3.3× 57 0.7× 58 0.7× 109 2.0× 11 471
Valentina Broshtilova Bulgaria 8 89 0.4× 69 0.7× 54 0.6× 77 0.9× 36 0.7× 44 347
Crystal Sung United States 11 102 0.5× 226 2.2× 96 1.1× 16 0.2× 132 2.4× 16 432
Parag Tamhankar India 10 95 0.4× 57 0.6× 20 0.2× 67 0.8× 36 0.7× 32 272
Gabriela Pasqualim Brazil 13 155 0.7× 258 2.6× 17 0.2× 64 0.8× 114 2.1× 31 397
Osvaldo Artigalás Brazil 13 120 0.5× 112 1.1× 9 0.1× 103 1.2× 64 1.2× 27 322

Countries citing papers authored by Christina Hung

Since Specialization
Citations

This map shows the geographic impact of Christina Hung's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Christina Hung with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christina Hung more than expected).

Fields of papers citing papers by Christina Hung

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christina Hung. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Christina Hung. The network helps show where Christina Hung may publish in the future.

Co-authorship network of co-authors of Christina Hung

This figure shows the co-authorship network connecting the top 25 collaborators of Christina Hung. A scholar is included among the top collaborators of Christina Hung based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Christina Hung. Christina Hung is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Hung, Christina, et al.. (2025). Kernel-level hidden rootkit detection based on eBPF. Computers & Security. 157. 104582–104582.
2.
Goldstein, Jennifer, Emily Groopman, Shruthi Mohan, et al.. (2024). Developing a scoring system for gene curation prioritization in lysosomal diseases. Molecular Genetics and Metabolism. 143(1-2). 108572–108572.
3.
Groopman, Emily, Shruthi Mohan, Raquel Fernández, et al.. (2024). Assessment of genes involved in lysosomal diseases using the ClinGen clinical validity framework. Molecular Genetics and Metabolism. 143(3). 108593–108593.
4.
Rashid, Asma, et al.. (2023). Multidisciplinary clinical and translational approach for optimizing management for complex and rare conditions using Kabuki syndrome as example. SHILAP Revista de lepidopterología. 1. 100008–100008. 3 indexed citations
5.
Jung, Youngsook L., Christina Hung, Jaejoon Choi, Eunjung Alice Lee, & Olaf A. Bodamer. (2023). Characterizing the molecular impact of KMT2D variants on the epigenetic and transcriptional landscapes in Kabuki syndrome. Human Molecular Genetics. 32(13). 2251–2261. 10 indexed citations
6.
Hartman, Deborah, et al.. (2022). From Genotype to Phenotype—A Review of Kabuki Syndrome. Genes. 13(10). 1761–1761. 26 indexed citations
7.
Potter, Sarah J., et al.. (2021). Lysine methyltransferase 2D regulates muscle fiber size and muscle cell differentiation. The FASEB Journal. 35(11). e21955–e21955. 11 indexed citations
8.
Rohanizadegan, Mersedeh, et al.. (2020). The tale of two genes: from next-generation sequencing to phenotype. Molecular Case Studies. 6(2). a004846–a004846. 2 indexed citations
9.
Wang, Yirou, Niu Li, Zhe Su, et al.. (2019). The phenotypic spectrum of Kabuki syndrome in patients of Chinese descent: A case series. American Journal of Medical Genetics Part A. 182(4). 640–651. 10 indexed citations
10.
Hung, Christina, et al.. (2019). Prenatal and perinatal history in Kabuki Syndrome. American Journal of Medical Genetics Part A. 182(1). 85–92. 7 indexed citations
11.
Hung, Christina, et al.. (2019). A novel FAM20C mutation causes a rare form of neonatal lethal Raine syndrome. American Journal of Medical Genetics Part A. 179(9). 1866–1871. 16 indexed citations
12.
Hung, Christina, James D. Baker, Johann Bauer, et al.. (2017). A defect in the inner kinetochore protein CENPT causes a new syndrome of severe growth failure. PLoS ONE. 12(12). e0189324–e0189324. 9 indexed citations
13.
Bodamer, Olaf A., et al.. (2017). Birth weight in patients with mucopolysaccharidosis type II: Data from the Hunter Outcome Survey (HOS). Molecular Genetics and Metabolism Reports. 11. 62–64. 5 indexed citations
14.
Rohanizadegan, Mersedeh, Anne O’Donnell‐Luria, Ivana Mihalek, et al.. (2017). Utility of rapid whole-exome sequencing in the diagnosis of Niemann–Pick disease type C presenting with fetal hydrops and acute liver failure. Molecular Case Studies. 3(6). a002147–a002147. 11 indexed citations
15.
Bodamer, Olaf A., et al.. (2014). The Diagnostic Path to Pompe Disease. European Neurological Review. 9(1). 83–83. 1 indexed citations
16.
Johnson, Britt, Hermann Mascher, Daniel Mascher, et al.. (2013). Analysis of Lyso-Globotriaosylsphingosine in Dried Blood Spots. Annals of Laboratory Medicine. 33(4). 274–278. 31 indexed citations
17.
Chien, Yin‐Hsiu, Olaf A. Bodamer, Shu‐Chuan Chiang, et al.. (2012). Lyso‐globotriaosylsphingosine (lyso‐Gb3) levels in neonates and adults with the Fabry disease later‐onset GLA IVS4+919G>A mutation. Journal of Inherited Metabolic Disease. 36(5). 881–885. 18 indexed citations
18.
Bodamer, Olaf A. & Christina Hung. (2010). Laboratory and genetic evaluation of Gaucher disease. Wiener Medizinische Wochenschrift. 160(23-24). 600–604. 24 indexed citations
19.
Orsini, Joseph J., Christina Hung, Monica Martin, et al.. (2010). Analysis of glucocerebrosidase activity in dry blood spots using tandem mass spectrometry. Clinica Chimica Acta. 412(3-4). 343–346. 17 indexed citations
20.
Ratschmann, Rene, Milen Minkov, Christina Hung, et al.. (2009). Transcobalamin II deficiency at birth. Molecular Genetics and Metabolism. 98(3). 285–288. 20 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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